Effects of intermittent hypoxia different regimes on mitochondrial lipid peroxidation and glutathione-redox balance in stressed rats

Central European Journal of Biology

Volumn 3, Issue 3, 2008, Pages 233-242

  Gonchar, Olga A ^a  

^a BOGOMOLETZ INSTITUTE OF PHYSIOLOGY   (Ukraine)

Author keywords

Adaptation; Antioxidant defense; Glutathione; Glutathione enzymes; Intermittent hypoxia; Lipid peroxidation; Mitochondria

Indexed keywords

RATTUS;

EID: 47349122917     PISSN: 1895104X     EISSN: 16443632     Source Type: Journal    
DOI: 10.2478/s11535-008-0016-7     Document Type: Article

References (44)

1. Lukyanova L.D., Novel approach to the understanding of molecular mechanisms of adaptation to hypoxia, In: Hargens A., Takeda N., Singal P. (Eds.), Adaptation Biology and Medicine, Current Concepts, New Delhi: Narosa, 2005
2. Clanton T.L., Klawitter P.F., Physiological and Genomic Consequences of Intermittent Hypoxia. Invited Review: Adaptive responses of skeletal muscle to intermittent hypoxia: the known and the unknown, J. Appl. Physiol., 2007, 90, 2476-2487
3. W.-Z. Zhu, Y. Xie, L. Chen, H.-T. Yang, Z.-N. Zhou, Intermittent high altitude hypoxia inhibits opening of mitochondrial permeability transition pores against reperfusion injury, J. Mol. Cell Cardiol., 2006, 40, 96-106
4. Vanden Hoek T.L., Becker L.B., Shao Z.H., Li C.Q., Schumacker P.T., Preconditioning in cardiomyocytes protects by attenuating oxidant stress at reperfusion, Circ. Res., 2000, 86, 541-548
5. Lin A.M., Dung S.W., Chen C.F., Ho L.T., Hypoxic preconditioning prevents cortical infarction by transient focal ischemia-reperfusion, Ann. N.Y. Acad. Sci., 2003, 993, 168-178
6. Sharp F., Ran R., Lu A., Tang Y., Strauss K., Glass T., et al., Hypoxic preconditioning protects against ischemic brain injury, Neuro Rx®, 2004, 1, 26-35
7. Gonchar O., Effect of intermittent hypoxia on proand antioxidant balance in rat heart during high-intensity chronic exercise, Acta Physiol. Hung., 2005, 92, 211-220
8. Yamashita N., Nishida M., Hoshida S., Kuzuya T., Hori M., Taniguchi N., et al., Induction of manganase superoxide dismutase in rat cardiac myocytes increases tolerance to hypoxia 24 hours after preconditioning, J. Clin. Invest., 1994, 94, 2193-2199
9. Zong P., Setty S., Sun W., Martinez R., Tune J., Ehrenburg I.V., et al., Intermittent hypoxic training protects canine myocardium from infarction, Exp. Biol. Med., 2004, 229, 806-812
10. Joyeux-Faure M., Stanke-Labesque F., Lefebvre B., Beguin P., Godin-Ribuot D., Ribuot C., et al., Chronic intermittent hypoxia increases infarction in the isolated rat heart, J. Appl. Physiol., 2005, 98, 1691-1696
11. Du G., Mouithys-Mickalad A., Sluse F., Generation of superoxide anion by mitochondria and impairment of their functions during anoxia and reoxygenation in vitro, Free Radic. Biol. Med., 1998, 25, 1066-1074
12. Schild L., Reiser G., Oxidative stress is involved in the permeabilization of the inner membrane of brain mitochondria exposed to hypoxia/reoxygenation and low micromolar Ca2+, FEBS J., 2005, 272, 3593-3601
13. Waypa G.B., Schumacker P.T., Hypoxic pulmonary vasoconstriction: redox events in oxygen sensing, J. Appl. Physiol., 2005, 98, 404-414
14. Schild L., Reinheckel T., Wiswedel I., Augustin W., Short-term impairment of energy production in isolated rat liver mitochondria by hypoxia/ reoxygenation: involvement of oxidative protein modification, Biochem. J., 1997, 328, 205-210
15. Bell E., Emerling B., Chandel N., Mitochondrial regulation of oxygen sensing, Mitochondrion, 2005, 5, 322-332
16. Jezek P., Hlavata L., Mitochondria in homeostasis of reactive oxygen species in cell, tissues, and organism, Int. J. Biochem. Cell Biol., 2005, 37, 2478-2503
17. Dickinson D.A., Forman H.J., Cellular glutathione and thiols metabolism, Biochem. Pharmacol., 2002, 64, 1019-1026
18. Arrigo A.P., Gene expression and the thiol redox state, Free Radic. Biol. Med., 1999, 27, 936-944
19. Vogel R., Wiesinger H., Hamprecht B., Dringen R., The regeneration of reduced glutathione in rat forebrain mitochondria identifies metabolic pathways providing the NADPH required, Neurosci. Lett., 1999, 275, 97-100
20. Jo S., Son M., Koh H., Lee S., Song I., Kim Y., et al., Control of mitochondrial redox balance and cellular defense against oxidative damage by mitochondrial NADP+-dependent isocitrate dehydrogenase, J. Biol. Chem., 2001, 276, 16168-16176
21. Mansfield K., Simon M., Keith B., Hypoxic reduction in cellular glutathione levels requires mitochondrial reactive oxygen species, J. Appl. Physiol., 2004, 97, 1358-1366
22. Jonson D., Lardy H., Isolation of liver and kidney mitochondria, Methods Enzymol., 1967,10, 94-96
23. Buege J., Aust S., Microsomal lipid peroxidation, Methods Enzymol., 1978, LII, 302-308
24. Drossos G., Lazou A., Panagopoulos Ph., Westaby S., Deferoxamine Cardioplegia reduces superoxide radical production in human myocardium, Ann. Thorac. Surg., 1995, 59, 169-172
25. Misra H., Fridovich I., The role of superoxide anion in the autoxidation of Epinephrine and a simple assay superoxide dismutase, J. Biol. Chem., 1972, 247, 3170-3175
26. Rotruck J.T., Pope A.L., Ganther H.E., Swanson A.B., Selenium: biochemical role as a component of glutathione peroxidase, Science, 1973, 179, 588-590
27. Warholm M., Guthenberg C., Bahr C., Mannervik B., Glutathione transferases from human liver, Methods Enzymol., 1985, 113, 499-501
28. Carlberg I., Mannervik B., Glutathione Reductase, Methods Enzymol., 1985, 113, 484-490
29. Putilina F.E., The NADP+-dependent isocitrate dehydrogenase activity determination, Methods Biochem., 1982, 1, 174-176
30. Anderson M., Determination of glutathione and glutathione disulfide in biological samples, Methods Enzymol., 1985, 113, 548-551
31. Halliwell B., Gutteridge J.M.C., Free radicals in Biology and Medicine, Oxford University Press, Oxford, 1999
32. Chandel N.S., Budinger S., The cellular basis for diverse responses to oxygen, Free Radic. Biol. Med., 2007, 42, 165-174
33. Yuan G., Adhikary G., McCormick A., Holcroft J., Kumar G., Prabhakar N., Role of oxidative stress in intermittent hypoxia-induced immediate early gene activation in rat PC12 cells, J. Physiol., 2004, 557, 773-783
34. Faraci F., Didion S., Vascular protection: superoxide dismutase isoforms in the vessel wall, Arterioscler. Thromb. Vasc. Biol., 2004, 24, 1367-1373
35. Jackson R.M., Parish G., Ho Y.S., Effects of hypoxia on expression of superoxide dismutase in cultured ATII cells and lung fibroblasts, Am. J. Physiol. Lung Cell Mol. Physiol., 1996, 271, L955-L962
36. MacMilan-Crow L.A., Crow J.P., Thompson J.A., Peroxynitrite-mediated inactivation of manganese superoxide dismutase involves nitration and oxidation of critical tyrosine residues, Biochemistry, 1998, 37, 1613-1622
37. Schild L., Reinheckel T., Reiser M., Horn T., Wolf G., Augustin W., Nitric oxide produced in rat liver mitochondria causes oxidative stress and impairment of respiration after transient hypoxia, FASEB J., 2003, 17, 2194-2201
38. Lacza Z., Puskar M., Figueroa J., Zhang J., Rajapakse N., Busija D., Mitochondrial nitric oxide synthase is constitutively active and is functionally upregulated in hypoxia, Free Radic. Biol. Med., 2001, 31, 1609-1615
39. Lluis J., Morales A., Blasco C., Colell A., Mari M., Garcia-Ruiz C., et al., Critical role of mitochondrial glutathione in the survival of hepatocytes during hypoxia, J. Biol. Chem., 2005, 280, 3224-3232
40. Arai M., Imai H., Koumura T., Yoshida M., Emoto K., Umeda M., et al., Mitochondrial phospholipids hydroperoxide glutathione peroxidase plays a major role in preventing oxidative injury to cells, J. Biol. Chem., 1999, 274, 4924-4933
41. Wispe J.R., Clark J.C., Bruhans M.S., Kropp K.E., Korfhagen T.R., Whitsett J.A., Synthesis and processing of the precursor for human manganosuperoxide dismutase, Biochim. Biophys. Acta., 1989, 994, 30-36
42. Lee S.M., Koh H.J., Park D.C., Song B.J., Huh T.L., Park J.W., Cytosolic NADP+-dependent isocitrate dehyrogenase status modulates oxidative damage to cells, Free Radic.Biol. Med., 2002, 32, 1185-1196
43. Wenger R.H., Cellular adaptation to hypoxia: O2-sensing protein hydroxylases, hypoxia-inducible transcription factors, and O2-regulated gene expression, FASEB J., 2002,16, 1151-1162
44. Zhai X., Zhou X., Aschraf M., Late ischemic preconditioning is mediated in myocytes by enhanced endogenous antioxidant activity stimulated by oxygen-derived free radicals, Ann. NY Acad. Sci., 1996, 793, 156-166